A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861289



Internal ID22636224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2759024..2762088hg38UCSC Ensembl
chr12:2868190..2871254hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg383065
hg193065
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460955, nssv17461182
Samples
Known GenesLOC283440
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861289
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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